Andreani A, Bonazzi D, Cavrini V, Gatti R, Giovanninetti G, Franchi L, Nanetti A
Farmaco Sci. 1977 Oct;32(10):703-12.
Thiosemicarbazones of N-alkyl-2-chloroindole-3-carboxaldehydes were synthesized and investigated for antiviral activity against RNA virus (parainfluenza type 3, HA-I/CR-8 stock) and DNA virus (vaccinia virus, HID stock). The effect of lipophilicity on the activity against vaccinia virus was considered. Relative lipophilicities were measured by a reversed phase thin-layer chromatographic technique. The most active compound N-isopropyl-2-chloroindole-3-carboxaldehyde thiosemicarbazone appeared comparable for its activity to methisazone.
合成了N-烷基-2-氯吲哚-3-甲醛缩氨基硫脲,并研究了其对RNA病毒(副流感3型,HA-I/CR-8毒株)和DNA病毒(痘苗病毒,HID毒株)的抗病毒活性。考虑了亲脂性对痘苗病毒活性的影响。通过反相薄层色谱技术测量相对亲脂性。活性最高的化合物N-异丙基-2-氯吲哚-3-甲醛缩氨基硫脲的活性与甲吲噻腙相当。